Suppr超能文献

无论透明质酸合成酶抑制剂活性如何,正常人内皮细胞中均不存在透明质酸合成,但在转化细胞中显著较高。

Hyaluronic acid synthesis is absent in normal human endothelial cells irrespective of hyaluronic acid synthetase inhibitor activity, but is significantly high in transformed cells.

作者信息

Amanuma K, Mitsui Y

机构信息

Cell Science and Technology Division, Fermentation Research Institute, Tsukuba City, Ibaraki, Japan.

出版信息

Biochim Biophys Acta. 1991 May 17;1092(3):336-40. doi: 10.1016/s0167-4889(97)90009-4.

Abstract

The characteristics of glycosaminoglycan (GAG) synthesis in normal and transformed human endothelial cells were analyzed by the incorporation of [3H]glucosamine and by the activities of GAG synthetases. The GAG synthesized by normal endothelial cells consisted of mainly heparan sulfate (HS) and chondroitin sulfate/dermatan sulfate but little hyaluronic acid (HA) (less than 1%). The characteristics of GAG synthesis by normal cells reflected the synthetic enzyme activities for each individual GAG: the activity of HA synthetase was very low. In spite of this, the activity of HA synthetase inhibitor, induced in growth-retarded fibroblasts with low HA synthetase activity (Matuoka et al. (1987 J. Cell Biol., 104, 1105-1115), was very low in endothelial cells. In contrast to normal cells, transformed endothelial (ECV304) cells synthesized mainly HA (62% of total GAGs). These findings suggest that the regulatory system of GAG metabolism is cell type specific, and that transformation is accompanied by high levels of HA synthesis in endothelial cells.

摘要

通过掺入[3H]葡糖胺以及糖胺聚糖(GAG)合成酶的活性,分析了正常和转化的人内皮细胞中GAG合成的特征。正常内皮细胞合成的GAG主要由硫酸乙酰肝素(HS)和硫酸软骨素/硫酸皮肤素组成,但透明质酸(HA)含量很少(不到1%)。正常细胞的GAG合成特征反映了每种GAG的合成酶活性:HA合成酶的活性非常低。尽管如此,在HA合成酶活性较低的生长迟缓成纤维细胞中诱导产生的HA合成酶抑制剂的活性(Matuoka等人,(1987年《细胞生物学杂志》,104卷,1105 - 1115页),在内皮细胞中非常低。与正常细胞相反,转化的内皮(ECV304)细胞主要合成HA(占总GAG的62%)。这些发现表明,GAG代谢的调节系统具有细胞类型特异性,并且转化伴随着内皮细胞中高水平的HA合成。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验